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Required Drug Substance (Viral Vaccine Experience)- Upstream /Downstream Processing of viral vaccines

Job Opportunity - Drug Substance (Viral Vaccine Experience) Bharat Biotech is looking for skilled professionals with hands-on experience in Drug Substance manufacturing for Viral Vaccines. Details are provided below  1. Location: Hyderabad 2. Experience: 2-6 Years 3. Key Skills & Experience Required a. Experience in Upstream /Downstream Processing of viral vaccines b. Operation and handling of bioreactors, fermenters, centrifuges, chromatography systems, filtration units c.  Knowledge of cell culture techniques (mammalian/avian cell lines)  d. Familiarity with aseptic techniques, GMP documentation, batch records e. Understanding of process optimization, scale-up, and technology transfer f. Exposure to in-process testing, troubleshooting, and equipment cleaning/sterilization g. Ability to work in a regulated, fast-paced manufacturing environment 4. How to Apply Interested candidates can share their updated CV to kiran4978@bharatbiotech.com Mention subject line as: Appl...
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Vacancy in Bioprocess Upstream & Downstream (Bacterial Vaccine Production) - B.Sc / M.Sc /B.Tech (Biotech, Microbiology, Biochemistry, or related)

Bharat Biotech International Limited for Bioprocess Production Team (Upstream & Downstream) at Genome Valley, Hyderabad.
If you or someone you know has relevant experience in vaccine or biopharma production,  you can apply!
Position: Bioprocess Upstream & Downstream (Bacterial Vaccine Production)
Location: Hyderabad
Experience: 3 to 8 years
Qualification: B.Sc / M.Sc /B.Tech (Biotech, Microbiology, Biochemistry, or related)
Apply at: "kiran4978@bharatbiotech.com"
Note: Suitable candidates will be contacted.
Key Responsibilities
Upstream Production:
Operation of bioreactors, fermenters, and incubators
Media preparation and cell culture handling
Monitoring pH, DO, temperature, agitation, etc.
Downstream Production:
Handling centrifuges, TFF systems, chromatography skids, and filtration units
Execution of purification processes (e.g., affinity, ion exchange)
Buffer preparation and CIP/SIP of equipment
General:
Documentation and compliance with GMP, SOPs, and safety protocols
Requirements Hands-on experience in vaccine/biopharma production processes
Knowledge of GMP, GDP, and cleanroom operations
Willing to work in shifts and controlled environments
Strong understanding of equipment and process parameters

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